Proposed Data Collection Submitted for Public Comment and Recommendations, 64470-64472 [2020-22490]
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Federal Register / Vol. 85, No. 198 / Tuesday, October 13, 2020 / Notices
the grantees’ work will be national,
regional approaches will be used to
develop new content and to test out
feasibility and acceptability of materials,
especially among healthcare providers
and medical societies.
CDC requests OMB approval to collect
program evaluation information from;
(1) healthcare practitioners from
disciplines targeted by each grantee,
including training participants, and (2)
health system staff.
Healthcare practitioners will complete
surveys to provide information on
whether project trainings impacted their
knowledge and practice behavior
regarding FASD
identification, prevention, and
treatment. The information will be used
to improve future trainings and assess
whether knowledge and practice
changes occurred. Some participants
will also complete qualitative key
informant interviews to gain additional
information on practice change. Health
system employees will be interviewed
or complete surveys as part of activities
to assess readiness of healthcare systems
to implement recommended practice
changes.
It is estimated that 16,938
respondents will participate in the
evaluation each year, for a total
estimated burden of 2,338 hours
annually. There are no costs to
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden per
response
(in hours)
Total
burden hours
Form name
Health Professionals .........................
FASD Core Training Participants .....
Health Professionals Survey ............
FASD Core Training Survey—PreTest.
FASD Core Training Survey—PostTest.
Health Professionals Survey (Nursing).
Key Informant Interviews with
Champions.
Medical Assistant—Pre-Test Survey
4013
4013
1
1
9/60
9/60
602
602
4013
1
5/60
335
667
1
9/60
101
14
2
45/60
21
334
1
10/60
56
Medical Assistant—Post-Test Survey.
Medical Assistants Change in Practice Survey.
Pre-Test Screening, Assessment,
and Diagnosis.
Post-Test Screening, Assessment,
and Diagnosis.
Pre-Test ND–PAE ............................
Post-Test ND–PAE ..........................
Pre-Test Treatment Across the Lifespan.
Post-Test Treatment Across the
Lifespan.
Social Work and Family Physicians
Pre-training Survey.
Social Work and Family Physicians
6-Month Follow Up Survey.
TCU Organizational Readiness Survey.
334
1
10/60
56
250
1
15/60
63
120
1
10/60
20
120
1
10/60
20
120
120
120
1
1
1
10/60
10/60
7/60
20
20
14
120
1
7/60
14
1167
1
8/60
156
1167
1
8/60
156
246
2
10/60
82
........................
........................
........................
2,338
FASD Core Training Participants .....
Nurses ...............................................
Nurses ...............................................
Certified Medical Assistants and students.
Certified Medical Assistants and students.
Certified Medical Assistants and students.
Pediatricians ......................................
Pediatricians ......................................
Pediatricians ......................................
Pediatricians ......................................
Pediatricians ......................................
Pediatricians ......................................
Family medicine physicians, social
workers, social work students.
Family medicine physicians, social
workers, social work students.
Health Systems Professionals ..........
Total ...........................................
...........................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2020–22492 Filed 10–9–20; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
BILLING CODE 4163–18–P
[60Day-21–0728; Docket No. CDC–2020–
0096]
khammond on DSKJM1Z7X2PROD with NOTICES
Number
responses
per
respondent
Type of respondents
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
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18:52 Oct 09, 2020
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The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled The National Notifiable Diseases
Surveillance System (NNDSS). The
NNDSS is the nation’s public health
surveillance system that monitors the
occurrence and spread of diseases and
SUMMARY:
E:\FR\FM\13OCN1.SGM
13OCN1
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 85, No. 198 / Tuesday, October 13, 2020 / Notices
conditions that are nationally notifiable
or under standard surveillance.
DATES: CDC must receive written
comments on or before December 14,
2020.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2020–
0096 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE MS–D74, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS–
D74, Atlanta, Georgia 30329; phone:
404–639–7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
VerDate Sep<11>2014
18:52 Oct 09, 2020
Jkt 253001
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
National Notifiable Diseases
Surveillance System (NNDSS) (OMB
Control No. 0920–0728, Exp. 4/30/
2023)—Revision—Center for
Surveillance, Epidemiology and
Laboratory Services (CSELS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Public Health Services Act (42
U.S.C. 241) authorizes CDC to
disseminate nationally notifiable
condition information. The National
Notifiable Diseases Surveillance System
(NNDSS) is based on data collected at
the state, territorial and local levels as
a result of legislation and regulations in
those jurisdictions that require health
care providers, medical laboratories,
and other entities to submit healthrelated data on reportable conditions to
public health departments. These
reportable conditions, which include
infectious and non-infectious diseases,
vary by jurisdiction depending upon
each jurisdiction’s health priorities and
needs. Each year, the Council of State
and Territorial Disease Epidemiologists
(CSTE), supported by CDC, determines
which reportable conditions should be
designated nationally notifiable or
under standardized surveillance.
CDC requests a three-year approval for
a Revision to the NNDSS (OMB Control
No. 0920–0728). This Revision includes
requests for approval to: (1) Receive case
notification data for Blastomycosis
which is now under standardized
surveillance; and (2) receive diseasespecific data elements for Carbon
Monoxide (CO) Poisoning, Congenital
Syphilis, and Sexually Transmitted
Disease (STD, not congenital).
The NNDSS currently facilitates the
submission and aggregation of case
notification data voluntarily submitted
to CDC from 60 jurisdictions: Public
health departments in every U.S. state,
New York City, Washington DC, five
U.S. territories (American Samoa, the
Commonwealth of Northern Mariana
Islands, Guam, Puerto Rico, and the U.S.
Virgin Islands), and three freely
associated states (Federated States of
PO 00000
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64471
Micronesia, the Republic of the
Marshall Islands, and the Republic of
Palau). This information is shared
across jurisdictional boundaries and
both surveillance and prevention and
control activities are coordinated at
regional and national levels.
Approximately 90% of case
notifications are encrypted and
submitted to NNDSS electronically from
already existing databases by automated
electronic messages. When automated
transmission is not possible, case
notifications are faxed, emailed,
uploaded to a secure network or entered
into a secure website. All case
notifications that are faxed, emailed,
and uploaded are done so in the form
of an aggregate weekly or annual report,
not individual cases. These different
mechanisms used to send case
notifications to CDC vary by the
jurisdiction and the disease or
condition. Private personally
identifiable information (PII) is
collected from automated electronic
messages and information can be
retrieved by PII. In addition, some
combinations of submitted data
elements could potentially be used to
identify individuals. Private information
is not be disclosed unless otherwise
compelled by law. All data are treated
in a secure manner consistent with the
technical, administrative, and
operational controls required by the
Federal Information Security
Management Act of 2002 (FISMA) and
the 2010 National Institute of Standards
and Technology (NIST) Recommended
Security Controls for Federal
Information Systems and Organizations.
Weekly tables of nationally notifiable
diseases are available through CDC
WONDER and data.cdc.gov. Annual
summaries of finalized nationally
notifiable disease data are published on
CDC WONDER and data.cdc.gov and
disease-specific data are published by
individual CDC programs.
The burden estimates include the
number of hours that the public health
department uses to process and send
case notification data from their
jurisdiction to CDC. Specifically, the
burden estimates include separate
burden hours incurred for automated
and non-automated transmissions,
separate weekly burden hours incurred
for modernizing surveillance systems as
part of NNDSS Modernization Initiative
(NMI) implementation, separate burden
hours incurred for annual data
reconciliation and submission, and
separate one-time burden hours
incurred for the addition of new
diseases and data elements. The burden
estimates for the one-time burden for
reporting jurisdictions for the addition
E:\FR\FM\13OCN1.SGM
13OCN1
64472
Federal Register / Vol. 85, No. 198 / Tuesday, October 13, 2020 / Notices
of case notification data for
Blastomycosis and disease-specific data
elements for CO Poisoning, Congenital
Syphilis, and Sexually Transmitted
Disease (not congenital). The estimated
annual burden for the 257 respondents
is 18,354 hours. The total burden hours
increased from 18,414 to 18,954 since
the last revision due to an increase in
diseases and disease-specific data
elements added in this revision as
compared to the last revision.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
States
States
States
States
States
.............................
.............................
.............................
.............................
.............................
Territories
Territories
Territories
Territories
Territories
.......................
.......................
.......................
.......................
.......................
Freely
Freely
Freely
Freely
Associated
Associated
Associated
Associated
States
States
States
States
Cities
Cities
Cities
Cities
Cities
..............................
..............................
..............................
..............................
..............................
Total ........................
Total burden
(in hours)
50
10
50
50
50
52
52
52
1
1
20/60
2
4
75
2
867
1,040
10,400
3,750
100
5
5
5
5
5
52
56
52
1
1
20/60
20/60
4
5
2
87
93
1,040
25
10
3
3
3
3
52
56
1
1
20/60
20/60
5
2
52
56
15
6
2
2
2
2
2
52
52
52
1
1
20/60
2
4
75
2
35
208
416
150
4
..............................................................................
........................
........................
........................
18,954
[FR Doc. 2020–22490 Filed 10–9–20; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–21–0109]
Agency Forms Undergoing Paperwork
Reduction Act Review
khammond on DSKJM1Z7X2PROD with NOTICES
Average
burden per
response
(in hours)
Weekly (Automated) ............................................
Weekly (Non-automated) .....................................
Weekly (NMI Implementation) .............................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Weekly (Automated) ............................................
Weekly, Quarterly (Non-automated) ....................
Weekly (NMI Implementation) .............................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Weekly (Automated) ............................................
Weekly, Quarterly (Non-automated) ....................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Weekly (Automated) ............................................
Weekly (Non-automated) .....................................
Weekly (NMI Implementation) .............................
Annual ..................................................................
One-time Addition of Diseases and Data Elements.
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Respiratory
Protective Devices—42 CFR 84—
Regulation to the Office of Management
and Budget (OMB) for review and
approval. CDC previously published a
‘‘Proposed Data Collection Submitted
for Public Comment and
Recommendations’’ notice on July 20,
2020 to obtain comments from the
public and affected agencies. CDC did
not receive comments related to the
VerDate Sep<11>2014
Number of
responses per
respondent
Number of
respondents
Form name
18:52 Oct 09, 2020
Jkt 253001
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
PO 00000
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Fmt 4703
Sfmt 4703
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Respiratory Protective Devices—42
CFR part 84—Regulation (OMB Control
No. 0920–0109, Exp. 10/31/2020) —
Revision — National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
E:\FR\FM\13OCN1.SGM
13OCN1
]]>Agencies
[Federal Register Volume 85, Number 198 (Tuesday, October 13, 2020)]
[Notices]
[Pages 64470-64472]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-22490]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-21-0728; Docket No. CDC-2020-0096]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed and/or
continuing information collection, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on a proposed
information collection project titled The National Notifiable Diseases
Surveillance System (NNDSS). The NNDSS is the nation's public health
surveillance system that monitors the occurrence and spread of diseases
and
[[Page 64471]]
conditions that are nationally notifiable or under standard
surveillance.
DATES: CDC must receive written comments on or before December 14,
2020.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2020-
0096 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (regulations.gov) or by U.S. mail to the address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS-D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email:
omb[email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses.
5. Assess information collection costs.
Proposed Project
National Notifiable Diseases Surveillance System (NNDSS) (OMB
Control No. 0920-0728, Exp. 4/30/2023)--Revision--Center for
Surveillance, Epidemiology and Laboratory Services (CSELS), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Public Health Services Act (42 U.S.C. 241) authorizes CDC to
disseminate nationally notifiable condition information. The National
Notifiable Diseases Surveillance System (NNDSS) is based on data
collected at the state, territorial and local levels as a result of
legislation and regulations in those jurisdictions that require health
care providers, medical laboratories, and other entities to submit
health-related data on reportable conditions to public health
departments. These reportable conditions, which include infectious and
non-infectious diseases, vary by jurisdiction depending upon each
jurisdiction's health priorities and needs. Each year, the Council of
State and Territorial Disease Epidemiologists (CSTE), supported by CDC,
determines which reportable conditions should be designated nationally
notifiable or under standardized surveillance.
CDC requests a three-year approval for a Revision to the NNDSS (OMB
Control No. 0920-0728). This Revision includes requests for approval
to: (1) Receive case notification data for Blastomycosis which is now
under standardized surveillance; and (2) receive disease-specific data
elements for Carbon Monoxide (CO) Poisoning, Congenital Syphilis, and
Sexually Transmitted Disease (STD, not congenital).
The NNDSS currently facilitates the submission and aggregation of
case notification data voluntarily submitted to CDC from 60
jurisdictions: Public health departments in every U.S. state, New York
City, Washington DC, five U.S. territories (American Samoa, the
Commonwealth of Northern Mariana Islands, Guam, Puerto Rico, and the
U.S. Virgin Islands), and three freely associated states (Federated
States of Micronesia, the Republic of the Marshall Islands, and the
Republic of Palau). This information is shared across jurisdictional
boundaries and both surveillance and prevention and control activities
are coordinated at regional and national levels.
Approximately 90% of case notifications are encrypted and submitted
to NNDSS electronically from already existing databases by automated
electronic messages. When automated transmission is not possible, case
notifications are faxed, emailed, uploaded to a secure network or
entered into a secure website. All case notifications that are faxed,
emailed, and uploaded are done so in the form of an aggregate weekly or
annual report, not individual cases. These different mechanisms used to
send case notifications to CDC vary by the jurisdiction and the disease
or condition. Private personally identifiable information (PII) is
collected from automated electronic messages and information can be
retrieved by PII. In addition, some combinations of submitted data
elements could potentially be used to identify individuals. Private
information is not be disclosed unless otherwise compelled by law. All
data are treated in a secure manner consistent with the technical,
administrative, and operational controls required by the Federal
Information Security Management Act of 2002 (FISMA) and the 2010
National Institute of Standards and Technology (NIST) Recommended
Security Controls for Federal Information Systems and Organizations.
Weekly tables of nationally notifiable diseases are available through
CDC WONDER and data.cdc.gov. Annual summaries of finalized nationally
notifiable disease data are published on CDC WONDER and data.cdc.gov
and disease-specific data are published by individual CDC programs.
The burden estimates include the number of hours that the public
health department uses to process and send case notification data from
their jurisdiction to CDC. Specifically, the burden estimates include
separate burden hours incurred for automated and non-automated
transmissions, separate weekly burden hours incurred for modernizing
surveillance systems as part of NNDSS Modernization Initiative (NMI)
implementation, separate burden hours incurred for annual data
reconciliation and submission, and separate one-time burden hours
incurred for the addition of new diseases and data elements. The burden
estimates for the one-time burden for reporting jurisdictions for the
addition
[[Page 64472]]
of case notification data for Blastomycosis and disease-specific data
elements for CO Poisoning, Congenital Syphilis, and Sexually
Transmitted Disease (not congenital). The estimated annual burden for
the 257 respondents is 18,354 hours. The total burden hours increased
from 18,414 to 18,954 since the last revision due to an increase in
diseases and disease-specific data elements added in this revision as
compared to the last revision.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
States......................................... Weekly (Automated)..................... 50 52 20/60 867
States......................................... Weekly (Non-automated)................. 10 52 2 1,040
States......................................... Weekly (NMI Implementation)............ 50 52 4 10,400
States......................................... Annual................................. 50 1 75 3,750
States......................................... One-time Addition of Diseases and Data 50 1 2 100
Elements.
Territories.................................... Weekly (Automated)..................... 5 52 20/60 87
Territories.................................... Weekly, Quarterly (Non-automated)...... 5 56 20/60 93
Territories.................................... Weekly (NMI Implementation)............ 5 52 4 1,040
Territories.................................... Annual................................. 5 1 5 25
Territories.................................... One-time Addition of Diseases and Data 5 1 2 10
Elements.
Freely Associated States....................... Weekly (Automated)..................... 3 52 20/60 52
Freely Associated States....................... Weekly, Quarterly (Non-automated)...... 3 56 20/60 56
Freely Associated States....................... Annual................................. 3 1 5 15
Freely Associated States....................... One-time Addition of Diseases and Data 3 1 2 6
Elements.
Cities......................................... Weekly (Automated)..................... 2 52 20/60 35
Cities......................................... Weekly (Non-automated)................. 2 52 2 208
Cities......................................... Weekly (NMI Implementation)............ 2 52 4 416
Cities......................................... Annual................................. 2 1 75 150
Cities......................................... One-time Addition of Diseases and Data 2 1 2 4
Elements.
---------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 18,954
--------------------------------------------------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2020-22490 Filed 10-9-20; 8:45 am]
BILLING CODE 4163-18-P
